Canonical Allele Identifier: PA179976
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 167000
ClinVar RCV Id: RCV000153157 RCV000271550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala3659Val
CA179975
NM_001277115.2:c.10976C>T